Other mutations in this stock |
Total: 87 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700008P02Rik |
A |
G |
3: 6,685,501 (GRCm39) |
|
probably benign |
Het |
Aadacl2 |
C |
T |
3: 59,917,997 (GRCm39) |
T82I |
probably benign |
Het |
Acadl |
T |
C |
1: 66,892,382 (GRCm39) |
N147S |
probably benign |
Het |
Actr3 |
A |
T |
1: 125,336,300 (GRCm39) |
M79K |
probably damaging |
Het |
Agbl3 |
A |
G |
6: 34,834,452 (GRCm39) |
S874G |
possibly damaging |
Het |
Aoah |
A |
T |
13: 21,187,118 (GRCm39) |
T472S |
probably damaging |
Het |
Asb16 |
A |
T |
11: 102,159,821 (GRCm39) |
D58V |
probably damaging |
Het |
B4galt1 |
T |
C |
4: 40,823,575 (GRCm39) |
D172G |
probably benign |
Het |
Bax |
T |
C |
7: 45,114,671 (GRCm39) |
N55S |
possibly damaging |
Het |
Bdkrb2 |
A |
G |
12: 105,558,118 (GRCm39) |
N120D |
possibly damaging |
Het |
Bicdl1 |
T |
C |
5: 115,789,325 (GRCm39) |
|
probably benign |
Het |
Cand1 |
A |
G |
10: 119,049,471 (GRCm39) |
L425P |
probably damaging |
Het |
Caskin1 |
G |
A |
17: 24,724,452 (GRCm39) |
|
probably null |
Het |
Cd248 |
C |
T |
19: 5,119,960 (GRCm39) |
P603S |
probably benign |
Het |
Cep95 |
G |
T |
11: 106,690,930 (GRCm39) |
R143L |
probably benign |
Het |
Clptm1l |
G |
T |
13: 73,762,792 (GRCm39) |
|
probably null |
Het |
Cntnap5a |
T |
C |
1: 115,987,930 (GRCm39) |
F154L |
possibly damaging |
Het |
Cyld |
A |
T |
8: 89,436,618 (GRCm39) |
I303F |
possibly damaging |
Het |
Dock2 |
A |
G |
11: 34,597,288 (GRCm39) |
S370P |
probably damaging |
Het |
Enah |
G |
T |
1: 181,749,858 (GRCm39) |
T327K |
probably damaging |
Het |
Farp2 |
A |
T |
1: 93,507,582 (GRCm39) |
S427C |
probably damaging |
Het |
Fbxw11 |
C |
T |
11: 32,683,612 (GRCm39) |
T301M |
probably damaging |
Het |
Foxc2 |
A |
T |
8: 121,843,915 (GRCm39) |
T188S |
probably benign |
Het |
Fzd2 |
A |
G |
11: 102,497,154 (GRCm39) |
T533A |
probably benign |
Het |
Glb1l2 |
G |
T |
9: 26,680,334 (GRCm39) |
S248* |
probably null |
Het |
Glul |
A |
T |
1: 153,781,284 (GRCm39) |
|
probably benign |
Het |
Gm28042 |
A |
G |
2: 119,871,887 (GRCm39) |
T946A |
probably benign |
Het |
Golga3 |
T |
A |
5: 110,329,649 (GRCm39) |
D2E |
probably damaging |
Het |
Grm1 |
A |
T |
10: 10,595,711 (GRCm39) |
F639Y |
probably benign |
Het |
Gzmn |
A |
G |
14: 56,403,368 (GRCm39) |
L247P |
probably benign |
Het |
Hgf |
T |
G |
5: 16,818,783 (GRCm39) |
I525R |
probably damaging |
Het |
Hnrnpul2 |
T |
A |
19: 8,808,696 (GRCm39) |
D719E |
probably benign |
Het |
Itga10 |
C |
T |
3: 96,559,054 (GRCm39) |
|
probably benign |
Het |
Itga9 |
T |
C |
9: 118,436,185 (GRCm39) |
|
probably null |
Het |
Itgb1 |
T |
A |
8: 129,431,939 (GRCm39) |
C16S |
probably damaging |
Het |
Itgb1 |
G |
T |
8: 129,431,940 (GRCm39) |
C16F |
possibly damaging |
Het |
Kat14 |
A |
G |
2: 144,236,020 (GRCm39) |
I251V |
probably benign |
Het |
Kdsr |
A |
T |
1: 106,662,271 (GRCm39) |
|
probably null |
Het |
Larp1b |
T |
C |
3: 40,987,909 (GRCm39) |
S44P |
probably damaging |
Het |
Lonp2 |
T |
C |
8: 87,399,700 (GRCm39) |
|
probably benign |
Het |
Lrp1 |
C |
T |
10: 127,441,475 (GRCm39) |
S216N |
probably benign |
Het |
Lrrc19 |
T |
C |
4: 94,529,187 (GRCm39) |
S32G |
probably benign |
Het |
Mdm2 |
G |
A |
10: 117,526,434 (GRCm39) |
T335M |
probably benign |
Het |
Mettl25 |
A |
G |
10: 105,615,493 (GRCm39) |
Y504H |
probably damaging |
Het |
Mill1 |
T |
C |
7: 17,979,572 (GRCm39) |
I13T |
probably benign |
Het |
Mmachc |
T |
A |
4: 116,560,721 (GRCm39) |
Q258L |
probably benign |
Het |
Mpdz |
T |
A |
4: 81,339,413 (GRCm39) |
I5L |
probably benign |
Het |
Mrps2 |
C |
T |
2: 28,359,500 (GRCm39) |
A119V |
probably benign |
Het |
Mtcl2 |
A |
T |
2: 156,869,557 (GRCm39) |
M1026K |
probably benign |
Het |
Mtmr11 |
A |
G |
3: 96,075,429 (GRCm39) |
T370A |
probably benign |
Het |
Nmi |
T |
C |
2: 51,848,989 (GRCm39) |
I34V |
possibly damaging |
Het |
Obscn |
A |
T |
11: 58,926,901 (GRCm39) |
M5538K |
possibly damaging |
Het |
Ogdhl |
T |
C |
14: 32,047,822 (GRCm39) |
I24T |
probably benign |
Het |
Omp |
G |
T |
7: 97,794,566 (GRCm39) |
D20E |
probably benign |
Het |
Or2ag19 |
A |
G |
7: 106,444,403 (GRCm39) |
Y195C |
possibly damaging |
Het |
Or52e8b |
A |
G |
7: 104,673,767 (GRCm39) |
V140A |
probably benign |
Het |
Or5b120 |
C |
T |
19: 13,480,121 (GRCm39) |
T138M |
probably benign |
Het |
Or6c69 |
A |
G |
10: 129,747,550 (GRCm39) |
V199A |
probably benign |
Het |
Otog |
A |
G |
7: 45,933,332 (GRCm39) |
H1291R |
probably benign |
Het |
Pgbd1 |
A |
G |
13: 21,607,462 (GRCm39) |
L244P |
probably damaging |
Het |
Ranbp2 |
A |
G |
10: 58,299,808 (GRCm39) |
I481V |
probably benign |
Het |
Rbp3 |
A |
T |
14: 33,677,749 (GRCm39) |
I566F |
probably damaging |
Het |
Rsph4a |
A |
G |
10: 33,781,525 (GRCm39) |
D125G |
probably benign |
Het |
Scn11a |
A |
G |
9: 119,598,873 (GRCm39) |
V1219A |
probably damaging |
Het |
Serpine3 |
G |
A |
14: 62,911,830 (GRCm39) |
G264D |
probably benign |
Het |
Slc4a10 |
T |
C |
2: 62,087,806 (GRCm39) |
F400L |
probably damaging |
Het |
Slco1a4 |
C |
T |
6: 141,791,173 (GRCm39) |
V8I |
probably benign |
Het |
Spen |
T |
C |
4: 141,215,335 (GRCm39) |
D499G |
unknown |
Het |
Stk32c |
A |
G |
7: 138,698,931 (GRCm39) |
|
probably null |
Het |
Tars1 |
A |
G |
15: 11,388,261 (GRCm39) |
V485A |
probably benign |
Het |
Tcerg1l |
A |
G |
7: 137,963,496 (GRCm39) |
L258P |
probably damaging |
Het |
Tmc2 |
A |
T |
2: 130,089,880 (GRCm39) |
I622F |
probably damaging |
Het |
Tmem183a |
A |
T |
1: 134,282,444 (GRCm39) |
N220K |
probably damaging |
Het |
Tnni3 |
T |
C |
7: 4,523,525 (GRCm39) |
D146G |
probably damaging |
Het |
Trappc11 |
G |
T |
8: 47,954,715 (GRCm39) |
D908E |
probably damaging |
Het |
Trappc8 |
A |
G |
18: 20,996,608 (GRCm39) |
Y436H |
probably damaging |
Het |
Ttc41 |
G |
A |
10: 86,612,254 (GRCm39) |
V1176I |
probably benign |
Het |
Ube2b |
A |
G |
11: 51,888,699 (GRCm39) |
V24A |
probably benign |
Het |
Usp30 |
T |
C |
5: 114,251,022 (GRCm39) |
C233R |
probably damaging |
Het |
Vmn1r87 |
T |
A |
7: 12,865,703 (GRCm39) |
T195S |
possibly damaging |
Het |
Vmn2r24 |
T |
C |
6: 123,783,479 (GRCm39) |
|
probably benign |
Het |
Vmn2r81 |
C |
A |
10: 79,128,858 (GRCm39) |
T583N |
probably damaging |
Het |
Vwa8 |
C |
T |
14: 79,145,670 (GRCm39) |
R116C |
probably damaging |
Het |
Wdr1 |
C |
A |
5: 38,687,315 (GRCm39) |
V239L |
probably benign |
Het |
Wdr17 |
C |
T |
8: 55,156,942 (GRCm39) |
|
probably benign |
Het |
Zfhx4 |
A |
C |
3: 5,306,789 (GRCm39) |
D5A |
probably damaging |
Het |
Zfyve27 |
T |
C |
19: 42,160,184 (GRCm39) |
|
probably null |
Het |
|
Other mutations in Kif12 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01306:Kif12
|
APN |
4 |
63,084,121 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01377:Kif12
|
APN |
4 |
63,088,962 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02232:Kif12
|
APN |
4 |
63,084,732 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02671:Kif12
|
APN |
4 |
63,088,694 (GRCm39) |
missense |
probably benign |
0.05 |
IGL02719:Kif12
|
APN |
4 |
63,086,033 (GRCm39) |
missense |
probably benign |
|
IGL03056:Kif12
|
APN |
4 |
63,085,193 (GRCm39) |
missense |
probably null |
0.00 |
ANU05:Kif12
|
UTSW |
4 |
63,089,660 (GRCm39) |
small insertion |
probably benign |
|
ANU23:Kif12
|
UTSW |
4 |
63,084,121 (GRCm39) |
missense |
probably damaging |
0.99 |
ANU74:Kif12
|
UTSW |
4 |
63,089,663 (GRCm39) |
frame shift |
probably null |
|
ANU74:Kif12
|
UTSW |
4 |
63,089,660 (GRCm39) |
small insertion |
probably benign |
|
IGL02984:Kif12
|
UTSW |
4 |
63,089,660 (GRCm39) |
small insertion |
probably benign |
|
R0401:Kif12
|
UTSW |
4 |
63,087,762 (GRCm39) |
splice site |
probably benign |
|
R0927:Kif12
|
UTSW |
4 |
63,087,010 (GRCm39) |
missense |
possibly damaging |
0.71 |
R2178:Kif12
|
UTSW |
4 |
63,085,196 (GRCm39) |
missense |
probably benign |
0.00 |
R2263:Kif12
|
UTSW |
4 |
63,087,758 (GRCm39) |
missense |
probably benign |
0.00 |
R2372:Kif12
|
UTSW |
4 |
63,086,796 (GRCm39) |
missense |
possibly damaging |
0.64 |
R2404:Kif12
|
UTSW |
4 |
63,088,790 (GRCm39) |
missense |
probably damaging |
1.00 |
R3903:Kif12
|
UTSW |
4 |
63,086,213 (GRCm39) |
missense |
possibly damaging |
0.73 |
R4126:Kif12
|
UTSW |
4 |
63,084,674 (GRCm39) |
missense |
probably benign |
0.00 |
R4271:Kif12
|
UTSW |
4 |
63,088,983 (GRCm39) |
missense |
probably benign |
0.39 |
R4386:Kif12
|
UTSW |
4 |
63,089,455 (GRCm39) |
missense |
probably damaging |
1.00 |
R4750:Kif12
|
UTSW |
4 |
63,086,020 (GRCm39) |
missense |
probably damaging |
0.99 |
R4945:Kif12
|
UTSW |
4 |
63,086,730 (GRCm39) |
critical splice donor site |
probably null |
|
R5177:Kif12
|
UTSW |
4 |
63,086,141 (GRCm39) |
missense |
probably benign |
0.13 |
R5421:Kif12
|
UTSW |
4 |
63,089,665 (GRCm39) |
missense |
probably benign |
0.40 |
R5644:Kif12
|
UTSW |
4 |
63,084,130 (GRCm39) |
missense |
possibly damaging |
0.75 |
R5757:Kif12
|
UTSW |
4 |
63,088,755 (GRCm39) |
missense |
probably damaging |
1.00 |
R5772:Kif12
|
UTSW |
4 |
63,084,178 (GRCm39) |
missense |
probably damaging |
1.00 |
R5858:Kif12
|
UTSW |
4 |
63,084,647 (GRCm39) |
missense |
probably benign |
0.04 |
R5929:Kif12
|
UTSW |
4 |
63,086,754 (GRCm39) |
missense |
probably damaging |
0.96 |
R6648:Kif12
|
UTSW |
4 |
63,089,554 (GRCm39) |
critical splice donor site |
probably null |
|
R7007:Kif12
|
UTSW |
4 |
63,084,717 (GRCm39) |
missense |
probably benign |
|
R7108:Kif12
|
UTSW |
4 |
63,089,442 (GRCm39) |
missense |
probably benign |
0.15 |
R7171:Kif12
|
UTSW |
4 |
63,086,931 (GRCm39) |
missense |
probably damaging |
1.00 |
R7852:Kif12
|
UTSW |
4 |
63,086,226 (GRCm39) |
missense |
probably benign |
0.13 |
R8532:Kif12
|
UTSW |
4 |
63,087,656 (GRCm39) |
nonsense |
probably null |
|
R9022:Kif12
|
UTSW |
4 |
63,090,121 (GRCm39) |
missense |
possibly damaging |
0.57 |
R9029:Kif12
|
UTSW |
4 |
63,087,704 (GRCm39) |
missense |
probably damaging |
1.00 |
R9052:Kif12
|
UTSW |
4 |
63,090,068 (GRCm39) |
missense |
probably damaging |
1.00 |
R9711:Kif12
|
UTSW |
4 |
63,084,126 (GRCm39) |
missense |
probably benign |
|
R9727:Kif12
|
UTSW |
4 |
63,085,978 (GRCm39) |
missense |
probably damaging |
1.00 |
RF011:Kif12
|
UTSW |
4 |
63,089,664 (GRCm39) |
small insertion |
probably benign |
|
RF031:Kif12
|
UTSW |
4 |
63,089,662 (GRCm39) |
small insertion |
probably benign |
|
RF036:Kif12
|
UTSW |
4 |
63,089,664 (GRCm39) |
small insertion |
probably benign |
|
RF039:Kif12
|
UTSW |
4 |
63,089,662 (GRCm39) |
small insertion |
probably benign |
|
RF041:Kif12
|
UTSW |
4 |
63,089,662 (GRCm39) |
small insertion |
probably benign |
|
T0975:Kif12
|
UTSW |
4 |
63,089,660 (GRCm39) |
small insertion |
probably benign |
|
Z1088:Kif12
|
UTSW |
4 |
63,089,660 (GRCm39) |
small insertion |
probably benign |
|
Z1176:Kif12
|
UTSW |
4 |
63,090,234 (GRCm39) |
missense |
possibly damaging |
0.95 |
Z1176:Kif12
|
UTSW |
4 |
63,089,660 (GRCm39) |
small insertion |
probably benign |
|
Z1177:Kif12
|
UTSW |
4 |
63,089,660 (GRCm39) |
small insertion |
probably benign |
|
|